Multi-layered sp2-bonded carbon tubes

ABSTRACT

A microstructure comprises a plurality of interconnected units wherein the units are formed of graphene tubes. The graphene tubes may be formed by photo-initiating the polymerization of a monomer in a pattern of units to form a polymer microlattice, removing unpolymerized monomer, coating the polymer microlattice with a metal, removing the polymer microlattice to leave a metal microlattice, depositing graphitic carbon on the metal microlattice, converting the graphitic carbon to graphene, and removing the metal microlattice. A ceramic may be deposited on the graphene and another graphene layer may be deposited on top of the ceramic to create a multi-layered sp 2 -bonded carbon tube.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Patent Application No. 62/611,483 filed on Dec. 28, 2017. This application is related to the application entitled “sp²-Bonded Carbon Structures” and having Attorney Docket No. TI-78907 filed concurrently herewith which claims priority to U.S. Provisional Patent Application No. 62/611,347 filed on Dec. 28, 2017, and to the application entitled “Hexagonal Boron Nitride Structures” and having Attorney Docket No. TI-78917 filed concurrently herewith which claims priority to U.S. Provisional Patent Application No. 62/611,499 filed on Dec. 28, 2017, and to the application entitled “Multi-Super Lattice For Switchable Arrays” and having Attorney Docket No. TI-78918 filed concurrently herewith, and to the application entitled “Filler Particles For Polymers” and having Attorney Docket No. TI-78919 filed concurrently herewith which claims priority to U.S. Provisional Patent Application No. 62/611,511 filed on Dec. 28, 2017, and to the application entitled “Gas Sensor With Superlattice Structure” and having Attorney Docket No. TI-78923 filed concurrently herewith which claims priority to U.S. Provisional Patent Application No. 62/611,554 filed on Dec. 29, 2017, the contents of which are hereby incorporated by reference in their entireties.

FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not Applicable

BACKGROUND

Graphene is a single-layer sp²-hybridized 2D network of carbon atoms that conceptually serves as the basis of many important allotropes of carbon. It can be stacked to form 3D graphite, rolled to form 1D carbon nanotubes, and fused to form 0D fullerenes. Owing to its strongly delocalized electron configuration, graphene exhibits exceptional charge carrier mobility, thermal conductivity, mechanical strength, and chemical stability. However, like other nanomaterials, the properties of graphene depend on its size, atomic structure, and physical environment. Graphene and graphene-based materials have tailorable properties that can be exploited in a broad range of devices, including transistors, capacitors, electron field emitters, transparent conductors, sensors, catalysts, and drug delivery agents. Other 2D crystals, most notably boron nitride and molybdenum disulfide, have also been isolated.

Two-dimensional (2D) sp²-bonded carbon exists in the form of graphene, buckyballs and carbon nanotubes (CNTs). Graphene is “flat” or 2D, fullerenes (“Buckyballs”) are spherical or 0D, and CNTs are tubes in 1D. Forming these materials in a singular, regular, repeatable structure has not previously been achieved. Superstructures of these materials may provide very strong, light, highly thermally and electrically conductive structures. Attempts have been made to fabricate sp²-bonded sponges as shown in FIG. 1A, however these structures are irregular with properties that vary with position.

The isolation of graphene via the mechanical exfoliation of graphite has sparked strong interest in two-dimensional (2D) layered materials. The properties of graphene include exceptional strength, and high electrical and thermal conductivity, while being lightweight, flexible and transparent. This opens the possibility of a wide range of potential applications, including high-speed transistors and sensors, barrier materials, solar cells, batteries, and composites.

Other classes of 2D materials of interest include transition metal dichalcogenide (TMDC) materials, hexagonal boron nitride (h-BN), as well as those based on Group 14 elements, such as silicene and germanene. The properties of these materials can range from semi-metallic, for example, NiTe₂ and VSe₂, to semiconducting, for example, WSe₂ and MoS₂, to insulating, for example, hexagonal boron nitride (h-BN).

Growth of regular 3D superstructures using sp²-bonded carbon may address the shortcomings of the flexible sp² carbons for 3D applications given that hexagonally arranged carbon is strong, chemically inert, electrically and thermally conductive, and optically transparent. Such 3D superstructures may find used in a number of applications from packaging, thin optically transparent electrically conductive strong thin films, and many more.

When a carbon atom is attached to three groups (or, as in the case of graphene, three other carbon atoms) and so is involved in three a bonds, it requires three orbitals in the hybrid set. This requires that it be sp² hybridized.

An sp²-hybridized bond has 33% s and 67% p character. The three sp² hybrid orbitals point towards the corners of a triangle at 120° to each other. Each sp² hybrid is involved in a σ bond. The remaining p orbital forms the π bond. A carbon double bond may be viewed as a σ+π bond.

BRIEF SUMMARY

In one example, a process for preparing multi-layered graphene tubes comprises: fabricating polymeric tubes having a microlattice structure using a self-propagating photopolymer waveguide technique to selectively photo-initiate polymerization in a photomonomer; depositing a metal coating on the polymer tubes by an electroless process; dissolving out the polymeric core leaving metal hollow tubes; growing graphene on the hollow metal tubes; etching away the metal using sulfuric acid (or any other suitable etchant) to leave graphene hollow tubes; depositing a dielectric ceramic (such as, e.g., alumina, zirconia, etc.) on the graphene using ALD deposition; and, growing graphene on the ceramic coating.

In an example, the graphene tubes are interconnected by chemical electronic bonds in contradistinction to the van der Waals forces that may cause carbon nanotubes (CNTs) to agglomerate.

In one example, a microstructure comprises a plurality of interconnected units wherein the units are formed of multi-layered graphene tubes. The microstructure may comprise a plurality of interconnected units including at least a first unit formed of first graphene tubes; and a second unit formed of second graphene tubes wherein one or more of the second graphene tubes are connected to one or more of the first graphene tubes. The multi-layered graphene tubes that form the microstructure may be arranged in an ordered structure and form symmetric patterns that repeat along the principal directions of three-dimensional space.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S)

FIG. 1A is a schematic drawing of a fabrication process for a metal-based microlattice template in accordance with an example.

FIG. 1B is a flowchart for the fabrication process depicted schematically in FIG. 1A.

FIG. 2 is a schematic diagram of a methodology for fabricating multi-layered, sp²-bonded carbon tubes.

DETAILED DESCRIPTION

It has been found that an organic/inorganic superstructure may be used as a template for the formation of a 3D metal superstructure that may then be used to grow graphitic carbon on the surface of the metal. The template may be fabricated through a self-propagating photopolymer waveguide technique (see, e.g., Xiaoyu Zheng et. al., Ultralight, Ultrastiff Mechanical Metamaterials; Science 344 (2014) 1373-1377 and T. A. Schaedler, et al., Ultralight Metallic Microlattices; Science 334 (2011) 962-965) in which an interconnected 3D photopolymer lattice may be produced upon exposure of an appropriate liquid photomonomer to collimated UV light through a specifically designed mask that contains openings with certain spacing and size. The fabricated microlattice may then be then coated by electroless copper or other suitable metal (e.g. Ni, Co, Au, Ag, Cu, and alloys thereof) followed by etching away the organic polymeric matrix (scaffold). The resulting metal-based microlattice may be then used as a template to grow the graphitic carbon. The thickness of the electroless plated metal may be controlled in the range of nanometer to micrometer by adjusting the plating time, temperature, and/or plating chemistry.

FIG. 1A schematically illustrates an exemplary fabrication process of organic polymeric microlattices (scaffolds) prior to coating with electroless plating.

The present disclosure is of a “periodically structured” carbon nanostructure. The carbon nanostructures of the prior art are irregular and have much larger dimensions than those which may be achieved using the methodology disclosed herein.

The present process may be used to create a regular array, and the superstructure dimensions (unit) and structure may be optimized for strength, thermal and other fundamental properties.

There are several aspects of this procedure that are noteworthy:

-   -   it provides a regular structure with defined dimensions;     -   it can form very thin metal (e.g. Ni, Co, Cu, Ag, Au)         microlattices;     -   it enables the formation of graphitic carbon on very thin metals         by a surface-limited process for very thin metal wires or tubes.

The present process uses a polymeric structure as a template for such fabrication with the subsequent formation of a metal superstructure that may then be exposed to a hydrocarbon (e.g. methane, ethylene, acetylene, benzene) to form graphitic carbon, followed by etching of the metal from under the graphitic carbon using appropriate etchants such as, for example, FeCl₃ or potassium permanganate.

Collimated light through a photomask or multi-photon lithography may be used in a photo-initiated polymerization to produce a polymer microlattice comprised of a plurality of units. Exemplary polymers include polystyrene and poly(methyl methacrylate) (PMMA). Once polymerized in the desired pattern, the remaining un-polymerized monomer may be removed.

The polymer structure (polymer scaffold) may then be plated with a suitable metal using an electroless plating process.

Electroless nickel plating (EN) is an auto-catalytic chemical technique that may be used to deposit a layer of nickel-phosphorus or nickel-boron alloy on a solid workpiece, such as metal, plastic, or ceramic. The process relies on the presence of a reducing agent, for example hydrated sodium hypophosphite (NaPO₂H₂.H₂O) which reacts with the metal ions to deposit metal. Alloys with different percentages of phosphorus, ranging from 2-5 (low phosphorus) to up to 11-14 (high phosphorus) are possible. The metallurgical properties of the alloys depend on the percentage of phosphorus.

Electroless plating has several advantages over electroplating. Free from flux-density and power supply issues, it provides an even deposit regardless of workpiece geometry, and with the proper pre-plate catalyst, may deposit on non-conductive surfaces. In contradistinction, electroplating can only be performed on electrically conductive substrates.

Before performing electroless plating, the material to be plated must be cleaned by a series of chemicals; this is known as the pre-treatment process. Failure to remove unwanted “soils” from the part's surface results in poor plating. Each pre-treatment chemical must be followed by water rinsing (normally two to three times) to remove chemicals that may adhere to the surface. De-greasing removes oils from surfaces, whereas acid cleaning removes scaling.

Activation may be done with an immersion into a sensitizer/activator solution—for example, a mixture of palladium chloride, tin chloride, and hydrochloric acid. In the case of non-metallic substrates, a proprietary solution is often used.

The pre-treatment required for the deposition of metals on a non-conductive surface usually consists of an initial surface preparation to render the substrate hydrophilic. Following this initial step, the surface may be activated by a solution of a noble metal, e.g., palladium chloride. Electroless bath formation varies with the activator. The substrate is then ready for electroless deposition.

The reaction is accomplished when hydrogen is released by a reducing agent, normally sodium hypophosphite (with the hydrogen leaving as a hydride ion) or thiourea, and oxidized, thus producing a negative charge on the surface of the part. The most common electroless plating method is electroless nickel plating, although silver, gold and copper layers can also be applied in this manner.

In principle any hydrogen-based reducing agent can be used although the redox potential of the reducing half-cell must be high enough to overcome the energy barriers inherent in liquid chemistry. Electroless nickel plating most often employs hypophosphite as the reducer while plating of other metals like silver, gold and copper typically makes use of low-molecular-weight aldehydes.

A benefit of this approach is that the technique can be used to plate diverse shapes and types of surfaces.

As illustrated in FIG. 1B, the organic polymeric microlattice may be electrolessly plated with metal followed by dissolving out the organic polymer scaffold. The resulting metal-based microlattice may then be coated with a thin layer of immersion tin to prevent the metal from oxidizing during the subsequent process which may include a heat treatment. Alternatively, the surface of the metal-based microlattice may be functionalized with appropriate functional groups to provide anchoring or reactions sites for subsequent interaction with a polymer matrix. A copper/nickel super-lattice may be used. The fabricated and surface-treated metal-based microlattice may be embedded within an organic polymeric matrix to fabricate an electrically or thermally or both an electrically and thermally conductive composite (see FIG. 2). Alternatively, the fabricated metal-based microlattice may be used as a template to synthesize a graphitic carbon superstructure. The metal may then be etched out to produce a graphene microstructure comprising a plurality of units wherein the units are formed of interconnected graphene tubes. The graphene tubes that form the microlattice may be arranged in an ordered structure and form symmetric patterns that repeat along the principal directions of three-dimensional space.

Referring now to FIG. 2, a process for fabricating multi-layered sp²-bonded carbon tubes is schematically illustrated, beginning in the upper, leftmost corner. A polymer matrix of units may be created as described above using collimated UV light, a digital mask and an UV-curable resin (photomonomer). An electroless plating process may then be used to deposit a metal (e.g. copper) on the surface of the polymer. The polymer may then be removed, leaving a metal tube upon which graphene may be formed. The metal may then be removed by e.g. chemical etching. A ceramic coating may then be deposited (e.g. by atomic layer deposition) on the sp²-bonded carbon. Another layer of sp²-bonded carbon may then be deposited on the exposed surface of the ceramic coating to create a multi-layered hexagonal boron nitride tube. Subsequently, additional layers of ceramic coating and sp²-bonded carbon may be similarly applied to create sp²-bonded carbon tubes with an even greater number of layers.

Modifications are possible in the described embodiments, and other embodiments are possible, within the scope of the claims. 

What is claimed is:
 1. A microstructure comprising: a plurality of interconnected units including at least a first unit formed of first tubes that comprise a first layer of graphene, a layer of ceramic on the first layer of graphene, and a second layer of graphene on a surface of the ceramic opposite the first layer of graphene; and a second unit formed of second graphene tubes that comprise a first layer of graphene, a layer of ceramic on the first layer of graphene, and a second layer of graphene on a surface of the ceramic opposite the first layer of graphene, wherein one or more of the second tubes are connected to one or more of the first tubes.
 2. The microstructure recited in claim 1 wherein the tubes are arranged in an ordered structure and form symmetric patterns that repeat along the principal directions of three-dimensional space.
 3. The microstructure recited in claim 1 wherein the tubes form a rigid structure.
 4. The microstructure recited in claim 1 wherein the plurality of units forms a microlattice.
 5. The microstructure recited in claim 1 wherein the tubes are hollow.
 6. The microstructure recited in claim 1 wherein the tubes comprise graphene tubes interconnected by chemical electronic bonds.
 7. A method of forming a multi-layered graphene microstructure comprising: photo-initiating the polymerization of a monomer in a pattern of units to form a polymer microlattice; removing unpolymerized monomer; coating the polymer microlattice with a metal; removing the polymer microlattice to leave a metal microlattice; depositing graphitic carbon on the metal microlattice; converting the graphitic carbon to a first graphene layer; removing the metal microlattice; depositing ceramic on the first graphene layer; depositing graphitic carbon on a surface of the ceramic opposite the first graphene layer; and converting the graphitic carbon to a second graphene layer.
 8. The method recited in claim 7 wherein photo-initiating the polymerization of the monomer comprises passing collimated light through a photomask.
 9. The method recited in claim 7 wherein photo-initiating the polymerization of the monomer comprises multi-photon lithography.
 10. The method recited in claim 7 wherein coating the polymer microlattice with a metal comprises the electroless deposition of copper.
 11. The method recited in claim 7 wherein coating the polymer microlattice with a metal comprises the electroless deposition of nickel.
 12. The method recited in claim 7 wherein the polymer microlattice comprises polystyrene.
 13. The method recited in claim 7 wherein the polymer microlattice comprises poly(methyl methacrylate).
 14. A multi-layered graphene microstructure prepared by the process comprising the steps of: photo-initiating the polymerization of a monomer in a pattern of units to form a polymer microlattice; removing unpolymerized monomer; coating the polymer microlattice with a metal; removing the polymer microlattice to leave a metal microlattice; depositing graphitic carbon on the metal microlattice; converting the graphitic carbon to a first graphene layer; removing the metal microlattice; depositing ceramic on the first graphene layer; depositing graphitic carbon on a surface of the ceramic opposite the first graphene layer; and converting the graphitic carbon to a second graphene layer.
 15. The multi-layered graphene microstructure recited in claim 14 wherein photo-initiating the polymerization of the monomer comprises passing collimated light through a photomask.
 16. The multi-layered graphene microstructure recited in claim 14 wherein photo-initiating the polymerization of the monomer comprises multi-photon lithography.
 17. The multi-layered graphene microstructure recited in claim 14 wherein coating the polymer microlattice with a metal comprises the electroless deposition of copper.
 18. The multi-layered graphene microstructure recited in claim 14 wherein coating the polymer microlattice with a metal comprises the electroless deposition of nickel.
 19. The multi-layered graphene microstructure recited in claim 14 wherein the polymer microlattice comprises polystyrene.
 20. The multi-layered graphene microstructure recited in claim 14 wherein the polymer microlattice comprises poly(methyl methacrylate). 